Past 3 months I’ve had an increase in pins and needles and tingling. It’s not fun! Is it all the time? Mines comes and goes.

Have a rant jolea that's what we're here for. Do you a ms nurse, bio bit not filled in so don't know where you are. My ms nurse reckons everyone with ms should be on a small dose of anti-depressants just because of the ms. Don't worry about being 'hooked' you won't be but they really help just to get a day with ms, might make a small difference and they all add up. Tingling us a pain in the but, I drop loads of things, live in the Potteries, mum worked for Wedgwood for 40 years, have more Wedgwood dinner services than you could throw a stick at, daren't use them because of dropping them, all replaced with plastic, know anyone who wants to buy a Wedgwood dinner service? There are ways round most things, take it from an old codger who has had to change loads of things in life. I still walk my Airedales, but on my mobility scooter, one on each arm, no hands involved cos they don't work. There is very little you can't do, have a boiler cos I can't deal with a kettle any more, special pegs for the washing line, Velcro on coats cos I don't do buttons or Zips etc., there are ways👏😍